Progressive myoclonus and histidinaemia
Identifieur interne : 006129 ( Main/Exploration ); précédent : 006128; suivant : 006130Progressive myoclonus and histidinaemia
Auteurs : J. S. Duncan [Royaume-Uni] ; P. Brown [Royaume-Uni] ; C. D. Marsden [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 1991.
Descripteurs français
- Pascal (Inist)
- Aminoacidopathie, Analyse biochimique, Association morbide, Electrodiagnostic, Electroencéphalographie, Etude cas, Exploration, Histidinémie, Homme, Maladie héréditaire, Mouvement involontaire, Myoclonie, Métabolisme pathologie, Potentiel évoqué somatosensoriel, Progressif, Système nerveux pathologie.
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Amino Acid Metabolism, Inborn Errors (blood), Amino Acid Metabolism, Inborn Errors (complications), Amino Acid Metabolism, Inborn Errors (physiopathology), Aminoacid disorder, Biochemical analysis, Case study, Cerebral Cortex (physiopathology), Concomitant disease, Electrodiagnosis, Electroencephalography, Evoked Potentials, Somatosensory (physiology), Exploration, Female, Genetic disease, Histidine (blood), Histidinemia, Human, Humans, Involuntary movement, Metabolic diseases, Myoclonus, Myoclonus (blood), Myoclonus (etiology), Myoclonus (physiopathology), Nervous system diseases, Progressive, Somatosensory evoked potential.
- MESH :
- chemical , blood : Histidine.
- blood : Amino Acid Metabolism, Inborn Errors, Myoclonus.
- complications : Amino Acid Metabolism, Inborn Errors.
- etiology : Myoclonus.
- physiology : Evoked Potentials, Somatosensory.
- physiopathology : Amino Acid Metabolism, Inborn Errors, Cerebral Cortex, Myoclonus.
- Adult, Female, Humans.
Url:
DOI: 10.1002/mds.870060119
Affiliations:
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Le document en format XML
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S." last="Duncan">J. S. Duncan</name><affiliation wicri:level="2"><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>University Department of Clinical Neurology, Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London</wicri:cityArea></affiliation></author><author><name sortKey="Brown, P" sort="Brown, P" uniqKey="Brown P" first="P." last="Brown">P. Brown</name><affiliation wicri:level="2"><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>University Department of Clinical Neurology, Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London</wicri:cityArea></affiliation></author><author><name sortKey="Marsden, C D" sort="Marsden, C D" uniqKey="Marsden C" first="C. D." last="Marsden">C. D. 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Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1991">1991</date><biblScope unit="vol">6</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="87">87</biblScope><biblScope unit="page" to="89">89</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">D975762136EAF73B64C658D040E27F33295A18B9</idno><idno type="DOI">10.1002/mds.870060119</idno><idno type="ArticleID">MDS870060119</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Amino Acid Metabolism, Inborn Errors (blood)</term><term>Amino Acid Metabolism, Inborn Errors (complications)</term><term>Amino Acid Metabolism, Inborn Errors (physiopathology)</term><term>Aminoacid disorder</term><term>Biochemical analysis</term><term>Case study</term><term>Cerebral Cortex (physiopathology)</term><term>Concomitant disease</term><term>Electrodiagnosis</term><term>Electroencephalography</term><term>Evoked Potentials, Somatosensory (physiology)</term><term>Exploration</term><term>Female</term><term>Genetic disease</term><term>Histidine (blood)</term><term>Histidinemia</term><term>Human</term><term>Humans</term><term>Involuntary movement</term><term>Metabolic diseases</term><term>Myoclonus</term><term>Myoclonus (blood)</term><term>Myoclonus (etiology)</term><term>Myoclonus (physiopathology)</term><term>Nervous system diseases</term><term>Progressive</term><term>Somatosensory evoked potential</term></keywords><keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Histidine</term></keywords><keywords scheme="MESH" qualifier="blood" xml:lang="en"><term>Amino Acid Metabolism, Inborn Errors</term><term>Myoclonus</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Amino Acid Metabolism, Inborn Errors</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Myoclonus</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Evoked Potentials, Somatosensory</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Amino Acid Metabolism, Inborn Errors</term><term>Cerebral Cortex</term><term>Myoclonus</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Female</term><term>Humans</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Aminoacidopathie</term><term>Analyse biochimique</term><term>Association morbide</term><term>Electrodiagnostic</term><term>Electroencéphalographie</term><term>Etude cas</term><term>Exploration</term><term>Histidinémie</term><term>Homme</term><term>Maladie héréditaire</term><term>Mouvement involontaire</term><term>Myoclonie</term><term>Métabolisme pathologie</term><term>Potentiel évoqué somatosensoriel</term><term>Progressif</term><term>Système nerveux pathologie</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader></TEI><affiliations><list><country><li>Royaume-Uni</li></country><region><li>Angleterre</li></region></list><tree><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Duncan, J S" sort="Duncan, J S" uniqKey="Duncan J" first="J. S." last="Duncan">J. S. Duncan</name></region><name sortKey="Brown, P" sort="Brown, P" uniqKey="Brown P" first="P." last="Brown">P. Brown</name><name sortKey="Marsden, C D" sort="Marsden, C D" uniqKey="Marsden C" first="C. D." last="Marsden">C. D. Marsden</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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